Regulatory and Clinical Consulting for the In-Vitro Diagnostics
By MARACA InternationalMARACA International is your partner for CE-marking and US Food and Drug Administration (FDA) submissions, delivering excellent service.
It has a vision to improve lives through service excellence and a mission to provide best-in-class regulatory, quality and clinical services to medical device (MD) and in-vitro diagnostic device (IVD) manufacturers, clinical laboratories, pharmaceutical companies and notified bodies.
MARACA brings more than 20 years' experience excellence for MD and IVDs.